A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502607



Internal ID18454202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1400514..1410591hg38UCSC Ensembl
Innerchr10:1442709..1452786hg19UCSC Ensembl
Innerchr10:1432709..1442786hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3810078
hg1910078
hg1810078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040953
Supporting Variants
Samples
Known GenesADARB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502607
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer